Autor: "Van Vught PW" - OpacWWW

Skocz do pozycji: 1.

Tytuł:: Gene expression profile of SOD1-G93A mouse spinal cord, blood and muscle.
Autorzy:: Saris CG; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Groen EJ
van Vught PW
van Es MA
Blauw HM
Veldink JH
van den Berg LH; Pokaż więcej
Źródło:: Amyotrophic lateral sclerosis & frontotemporal degeneration [Amyotroph Lateral Scler Frontotemporal Degener] 2013 Apr; Vol. 14 (3), pp. 190-8. Date of Electronic Publication: 2013 Jan 08.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Gene Expression Profiling/*methods
Muscle, Skeletal/*enzymology
Spinal Cord/*enzymology
Superoxide Dismutase/*blood
Superoxide Dismutase/*genetics
Age Factors ; Animals ; Female ; Humans ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic ; Superoxide Dismutase/metabolism

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Skocz do pozycji: 2.

Tytuł:: EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans.
Autorzy:: Van Hoecke A; Laboratory of Neurobiology, Vesalius Research Center, VIB, Leuven, Belgium.
Schoonaert L
Lemmens R
Timmers M
Staats KA
Laird AS
Peeters E
Philips T
Goris A
Dubois B
Andersen PM
Al-Chalabi A
Thijs V
Turnley AM
van Vught PW
Veldink JH
Hardiman O
Van Den Bosch L
Gonzalez-Perez P
Van Damme P
Brown RH Jr
van den Berg LH
Robberecht W; Pokaż więcej
Źródło:: Nature medicine [Nat Med] 2012 Sep; Vol. 18 (9), pp. 1418-22.
Typ publikacji:: Journal Article; Research Support, American Recovery and Reinvestment Act; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Phenotype*
Amyotrophic Lateral Sclerosis/*physiopathology
Motor Neurons/*pathology
Receptor, EphA4/*metabolism
Signal Transduction/*physiology
Superoxide Dismutase/*metabolism
Amyotrophic Lateral Sclerosis/metabolism ; Analysis of Variance ; Animals ; Base Sequence ; Gene Knockdown Techniques ; Humans ; Mice ; Mice, Knockout ; Molecular Sequence Data ; Morpholinos/genetics ; Motor Neurons/metabolism ; Rats ; Rotarod Performance Test ; Sequence Analysis, DNA ; Statistics, Nonparametric ; Superoxide Dismutase-1 ; Zebrafish

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Skocz do pozycji: 3.

Tytuł:: Mapping of gene expression reveals CYP27A1 as a susceptibility gene for sporadic ALS.
Autorzy:: Diekstra FP; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Saris CG
van Rheenen W
Franke L
Jansen RC
van Es MA
van Vught PW
Blauw HM
Groen EJ
Horvath S
Estrada K
Rivadeneira F
Hofman A
Uitterlinden AG
Robberecht W
Andersen PM
Melki J
Meininger V
Hardiman O
Landers JE
Brown RH Jr
Shatunov A
Shaw CE
Leigh PN
Al-Chalabi A
Ophoff RA
van den Berg LH
Veldink JH; Pokaż więcej
Źródło:: PloS one [PLoS One] 2012; Vol. 7 (4), pp. e35333. Date of Electronic Publication: 2012 Apr 11.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Gene Expression Profiling*
Genome-Wide Association Study*
Amyotrophic Lateral Sclerosis/*genetics
Cholestanetriol 26-Monooxygenase/*genetics
Quantitative Trait Loci/*genetics
Genetic Predisposition to Disease ; Genotype ; HapMap Project ; Humans ; Linkage Disequilibrium ; Motor Neurons/pathology ; Pedigree ; Polymorphism, Single Nucleotide ; Xanthomatosis, Cerebrotendinous/genetics

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Skocz do pozycji: 4.

Tytuł:: Multifocal motor neuropathy is not associated with genetic variation in PTPN22, BANK1, Blk, FCGR2B, CD1A/E, and TAG-1 genes.
Autorzy:: Vlam L; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Cats EA
Seelen M
van Vught PW
van den Berg LH
van der Pol WL; Pokaż więcej
Źródło:: Journal of the peripheral nervous system : JPNS [J Peripher Nerv Syst] 2011 Sep; Vol. 16 (3), pp. 175-9.
Typ publikacji:: Journal Article
MeSH Terms:: Genetic Predisposition to Disease/*genetics
Polyneuropathies/*genetics
Polyneuropathies/*immunology
Adaptor Proteins, Signal Transducing/genetics ; Adult ; Aged ; Antigens, CD1/genetics ; Contactin 2/genetics ; Female ; Genotype ; Humans ; Male ; Membrane Proteins/genetics ; Middle Aged ; Polymerase Chain Reaction ; Polymorphism, Single Nucleotide ; Protein Tyrosine Phosphatase, Non-Receptor Type 22/genetics ; Receptors, IgG/genetics ; src-Family Kinases/genetics

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Skocz do pozycji: 5.

Tytuł:: Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.
Autorzy:: van Es MA; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Veldink JH
Saris CG
Blauw HM
van Vught PW
Birve A
Lemmens R
Schelhaas HJ
Groen EJ
Huisman MH
van der Kooi AJ
de Visser M
Dahlberg C
Estrada K
Rivadeneira F
Hofman A
Zwarts MJ
van Doormaal PT
Rujescu D
Strengman E
Giegling I
Muglia P
Tomik B
Slowik A
Uitterlinden AG
Hendrich C
Waibel S
Meyer T
Ludolph AC
Glass JD
Purcell S
Cichon S
Nöthen MM
Wichmann HE
Schreiber S
Vermeulen SH
Kiemeney LA
Wokke JH
Cronin S
McLaughlin RL
Hardiman O
Fumoto K
Pasterkamp RJ
Meininger V
Melki J
Leigh PN
Shaw CE
Landers JE
Al-Chalabi A
Brown RH Jr
Robberecht W
Andersen PM
Ophoff RA
van den Berg LH; Pokaż więcej
Źródło:: Nature genetics [Nat Genet] 2009 Oct; Vol. 41 (10), pp. 1083-7. Date of Electronic Publication: 2009 Sep 06.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Chromosomes, Human, Pair 9*
Genome-Wide Association Study*
Polymorphism, Single Nucleotide*
Amyotrophic Lateral Sclerosis/*genetics
Chromosomes, Human, Pair 19 ; Disease Susceptibility ; Genome, Human ; Humans

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Skocz do pozycji: 6.

Tytuł:: Analysis of FGGY as a risk factor for sporadic amyotrophic lateral sclerosis.
Autorzy:: Van Es MA; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Centre Utrecht, Heidelbergaan 100, Utrecht, The Netherlands.
Van Vught PW
Veldink JH
Andersen PM
Birve A
Lemmens R
Cronin S
Van Der Kooi AJ
De Visser M
Schelhaas HJ
Hardiman O
Ragoussis I
Lambrechts D
Robberecht W
Wokke JH
Ophoff RA
Van Den Berg LH; Pokaż więcej
Źródło:: Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases [Amyotroph Lateral Scler] 2009 Oct-Dec; Vol. 10 (5-6), pp. 441-7.
Typ publikacji:: Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Predisposition to Disease*
Genetic Variation*
Amyotrophic Lateral Sclerosis/*genetics
Proteins/*genetics
Europe ; Female ; Genetics, Population ; Genome, Human ; Genome-Wide Association Study ; Humans ; Male ; Polymorphism, Single Nucleotide ; Population Groups ; Risk Factors

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Skocz do pozycji: 7.

Tytuł:: Weighted gene co-expression network analysis of the peripheral blood from Amyotrophic Lateral Sclerosis patients.
Autorzy:: Saris CG; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht 3584 CX, the Netherlands. />Horvath S
van Vught PW
van Es MA
Blauw HM
Fuller TF
Langfelder P
DeYoung J
Wokke JH
Veldink JH
van den Berg LH
Ophoff RA; Pokaż więcej
Źródło:: BMC genomics [BMC Genomics] 2009 Aug 27; Vol. 10, pp. 405. Date of Electronic Publication: 2009 Aug 27.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Gene Expression Profiling*
Amyotrophic Lateral Sclerosis/*genetics
Adult ; Aged ; Amyotrophic Lateral Sclerosis/blood ; Case-Control Studies ; Cluster Analysis ; Female ; Genome, Human ; Humans ; Male ; Middle Aged ; RNA, Messenger/genetics ; Young Adult

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Skocz do pozycji: 8.

Tytuł:: Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.
Autorzy:: van Es MA; Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht 3584 CX, The Netherlands.
van Vught PW
Blauw HM
Franke L
Saris CG
Van den Bosch L
de Jong SW
de Jong V
Baas F
van't Slot R
Lemmens R
Schelhaas HJ
Birve A
Sleegers K
Van Broeckhoven C
Schymick JC
Traynor BJ
Wokke JH
Wijmenga C
Robberecht W
Andersen PM
Veldink JH
Ophoff RA
van den Berg LH; Pokaż więcej
Źródło:: Nature genetics [Nat Genet] 2008 Jan; Vol. 40 (1), pp. 29-31. Date of Electronic Publication: 2007 Dec 16.
Typ publikacji:: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
MeSH Terms:: Genetic Predisposition to Disease*
Amyotrophic Lateral Sclerosis/*genetics
Nerve Tissue Proteins/*genetics
Peptide Hydrolases/*genetics
Potassium Channels/*genetics
Case-Control Studies ; Chromosomes, Human, Pair 7 ; Dipeptidyl-Peptidases and Tripeptidyl-Peptidases ; Humans ; Polymorphism, Single Nucleotide ; White People/genetics

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